KIF18A

kinesin family member 18A

Summary

KIF18A is a member of the kinesin superfamily of microtubule-associated molecular motors (see MIM 148760) that use hydrolysis of ATP to produce force and movement along microtubules (Luboshits and Benayahu, 2005 [PubMed 15878648]).[supplied by OMIM, Aug 2008]

Known Variants47 total

rsidPosition (GRCh37)AllelesClassClinVar
rs132076559711:28,042,788T/C—uncertain significance
rs75154800911:28,042,796C/T—likely benign
rs13997232611:28,042,799G/A—conflicting classifications of pathogenicity
rs19951261311:28,045,363T/G—uncertain significance
rs3544065711:28,045,367G/A—likely benign
rs57645118111:28,049,720C/T——
rs147698759111:28,057,803T/A—uncertain significance
rs76477940011:28,057,844T/C—uncertain significance
rs213349638811:28,057,870C/T—uncertain significance
rs249426226911:28,057,882C/T—uncertain significance
rs249426258111:28,057,947T/A—uncertain significance
rs14265684211:28,057,992A/G—uncertain significance
rs15018487011:28,058,010G/A—uncertain significance
rs249426293111:28,058,034T/C—uncertain significance
rs13874181011:28,058,043G/A—uncertain significance
rs14937184711:28,058,052A/G—uncertain significance
rs54613705111:28,058,058T/C—uncertain significance
rs120114880911:28,058,121T/C—uncertain significance
rs77597037911:28,058,144C/T—uncertain significance
rs748265011:28,074,833T/Gupstream gene variant—
rs249429865211:28,080,486C/G—uncertain significance
rs95322660211:28,080,535A/G—likely benign
rs18370094211:28,080,626A/T—uncertain significance
rs249429919311:28,080,641T/G—uncertain significance
rs249429927811:28,080,670T/C—uncertain significance
rs185086836111:28,084,027G/A—uncertain significance
rs37361950411:28,090,816T/C—uncertain significance
rs123410907411:28,090,820C/T—uncertain significance
rs76779875511:28,090,909T/C—uncertain significance
rs76574847111:28,090,927C/T—uncertain significance
rs249432771711:28,098,555T/G—uncertain significance
rs77737150911:28,104,769C/T—uncertain significance
rs37613972011:28,106,212C/G—uncertain significance
rs249433985211:28,106,243A/G—uncertain significance
rs77994667111:28,106,273A/G—uncertain significance
rs37567095211:28,110,163C/T—likely benign
rs77189152111:28,110,165G/C—uncertain significance
rs76666279211:28,110,220G/A—uncertain significance
rs132805560711:28,112,214G/A—uncertain significance
rs37341528611:28,113,026T/C—uncertain significance
rs75825841211:28,116,210T/C—uncertain significance
rs117461947511:28,116,217T/C—uncertain significance
rs76247389311:28,119,206T/C—uncertain significance
rs75747420711:28,119,253T/G—uncertain significance
rs75053878711:28,119,281G/A—uncertain significance
rs74803128211:28,119,297C/G—uncertain significance
rs185139701311:28,119,485T/G—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.